To Do


updates Jan2012

posted Jan 5, 2012, 1:21 PM by Christoph Lossin   [ updated Jan 5, 2012, 1:28 PM ]

switch navigation to:
Exons (coding)
Introns
5'UTR
3'UTR
Promoter
take out the Polymorphisms sub and enter it with other appropriate variations
include rs# for SNPs
update statistics
mutation > variation

enter rs link via http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=4131162

Mutations from SfN2010

posted Mar 28, 2011, 2:14 PM by Christoph Lossin, Ph.D.

M1438T
N1735K
by *Y. LIAO et al, SfN2010

NG and NM files

posted Dec 14, 2010, 12:29 PM by Christoph Lossin, Ph.D.   [ updated Dec 14, 2010, 12:30 PM ]


NG_011906.1
NM_006920.4 (-33)

Reference hyperlink cleanup

posted Oct 26, 2010, 6:50 AM by Christoph Lossin, Ph.D.

We ought to clean up the hyperlinks in the References web page from redundancy. A straight PMID link ought to be used.

SCN1A promoter?

posted Oct 25, 2010, 4:05 PM by Christoph Lossin, Ph.D.

check martin 2007 for SCN1A promoter

Mancardi 2006... errors!

posted Oct 25, 2010, 2:55 PM by Christoph Lossin, Ph.D.

recheck all reports in Mancardi et al, Epilepsia 47:1629 (2006)

Phosphorylation

posted Oct 25, 2010, 9:47 AM by Christoph Lossin, Ph.D.

incorporate references into reference page

MAT update

posted Oct 25, 2010, 9:07 AM by Christoph Lossin, Ph.D.

MAT has a bug in "Deletion" where it incorrectly states off-frame codonic deletions (multiples of 3)

Hyperlinks

posted Oct 25, 2010, 7:35 AM by Christoph Lossin, Ph.D.

update hyperlinks in non-coding, genomic, and Reference page itself

Urgent items

posted Oct 23, 2010, 11:24 AM by Christoph Lossin, Ph.D.   [ updated Oct 23, 2010, 5:54 PM ]

Update total statistics

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